Lung NodulesNCT07448441
Clinical Study of Trap-(FAPI)3 PET Imaging in the Diagnosis of Pulmonary Nodules
An observational study of Lung Nodules, run by Daping Hospital and the Research Institute of Surgery of the Third Military Medical University at 1 site in China.
Trial summary
The excellent tumor-targeting efficacy of FAP has been confirmed by multiple clinical studies. The results unequivocally establish FAPI as a tumor-targeting ligand with significant potential, demonstrating important application prospects in translational oncology. Read more about this study
- Who is it for?
- Ages 18 to 65 years
- Conditions the study is for
- Lung Nodules
- How many people
- 50 participants
- Where
- 1 siteChina
- Study dates
- 1 Mar 2026to 31 Dec 2027
- Phase
- Observational
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 65 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: The subjects we selected are adults who are not restricted by gender. Fordetails, please refer to the "EligibilityCriteria" colymn.
Who may be able to join
- 1) Patients aged over 18 years with no gender restriction;
- 2) Patients with radiographic findings of pulmonary nodules;
- 3) Patients eligible for Trap-(FAPI)3 PET examination;
- 4) Written informed consent signed by the subject or their legal guardian.
Who cannot join
- 1) Patients who have received antitumor therapy prior to PET/CT scanning;
- 2) Patients with severe diseases that cannot tolerate PET/CT scanning;
- 3) Alternative subjects with contraindications to PET/CT scanning;
- 4) Radiation exposure exceeding 50 mSv dose in the past year;
- 5) Alternative subjects who underwent major surgery within the past 3 months; those who received experimental drugs or devices (with unclear efficacy or safety) within the past 1 month;
- 6) Alternative subjects with any clinical conditions that the principal investigator of this study considers may cause or pose potential hazards from the investigational product.
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
China1 site
Department of Nuclear Medicine, Daping Hospital of Army Medical University
Chongqing, Chongqing Municipality, 400010
About this study
The excellent tumor-targeting efficacy of FAP has been confirmed by multiple clinical studies. The results unequivocally establish FAPI as a tumor-targeting ligand with significant potential, demonstrating important application prospects in translational oncology. However, its therapeutic effects remain under investigation. An ideal radiopharmaceutical for cancer treatment should possess outstanding targeting specificity and relatively prolonged tumor retention time. Previous studies have shown that radiolabeled FAPI variants (FAPI-04 and FAPI-46) rapidly and satisfactorily accumulate in tumors, while exhibiting low physiological uptake in normal tissues. However, prior FAP-related tracers demonstrated relatively short retention times in small pulmonary lesions. Our aim is to design a FAPI trimer, Trap-(FAPI)3, to optimize pharmacokinetics and evaluate whether this novel drug offers superior advantages over its monomer analogs in the imaging diagnosis and staging of pulmonary tumors.
Read the detailed description
Positron Emission Tomography (PET) is a functional imaging technology for the diagnosis and monitoring of tumors. The clinical applications of PET in malignant tumors, including staging, response evaluation, and efficacy prediction, provide attractive semi-quantitative biomarkers for clinical and research platforms. Understanding the advantages and limitations of fundamental imaging science and imaging modalities is crucial for optimizing research evaluations. With the widespread use of functional techniques and the development of novel PET biomarkers, PET research evaluations will be further improved.
The field of oncology has undergone a revolution due to molecular imaging, which evaluates tumor biology, while traditional radiological imaging focuses on morphological anatomy. Molecular imaging employs non-invasive visualization of physiological or pathological processes at the cellular or subcellular level. Positron Emission Tomography/Computed Tomography (PET/CT) is a hybrid imaging tool that provides complementary information on both function and structure. [18F]Fluorodeoxyglucose (FDG), first developed in the late 1970s as a tracer for brain metabolism, is now the most widely used PET tracer with applications in both oncological and non-oncological pathways. Although its clinical utility is undeniable, FDG uptake serves as a surrogate indicator for glucose transport/metabolism and is not specific to malignant tumors. The diagnostic accuracy of FDG for pulmonary nodules has long been a challenge, as tumor cells are scarce, solid components are minimal, and mucinous components are excessive. Multiple factors can lead to low uptake or no uptake of pulmonary nodules.
Through continuous exploration of cellular targets, fibroblast-activating protein (FAP) was identified. Cancer-associated fibroblasts are present in numerous tumors, particularly those with strong fibroblast proliferation responses, such as breast cancer, colorectal cancer, pancreatic cancer, prostate cancer, and lung cancer. Consequently, FAP expression is detected in over 90% of epithelial tumors. To date, FAP expression has been reported to correlate with poor tumor prognosis, as observed in colorectal cancer, pancreatic cancer, hepatocellular carcinoma, and ovarian cancer. Although further research is required, this advantage positions cancer-associated fibroblasts as an ideal target for antitumor therapy. In practical applications, low FAP expression in fibroblasts or healthy tissues facilitates imaging of pathological changes with low background signals.
Cancer-associated fibroblasts (CAFs) are key components of the tumor microenvironment, accounting for over half of the mass in various types of tumors. Previous studies have demonstrated that CAFs play significant roles in tumor growth, immunosuppression, and cancer invasion. Consequently, CAFs may emerge as a novel therapeutic target for lung tumor diagnosis and treatment. Fibroblast-activating protein (FAP) is overexpressed in CAFs of multiple epithelial cancers but weakly expressed in healthy tissues, making it an attractive target in cancer research. In recent years, molecular imaging targeting FAP has been extensively explored in the field of tumor diagnosis.
The excellent tumor-targeting efficacy of FAP has been confirmed by multiple clinical studies. The results unequivocally establish FAPI as a tumor-targeting ligand with significant potential, demonstrating important application prospects in translational oncology. However, its therapeutic effects remain under investigation. An ideal radiopharmaceutical for cancer treatment should possess outstanding targeting specificity and relatively prolonged tumor retention time. Previous studies have shown that radiolabeled FAPI variants (FAPI-04 and FAPI-46) rapidly and satisfactorily accumulate in tumors, while exhibiting low physiological uptake in normal tissues. However, prior FAP-related tracers demonstrated relatively short retention times in small pulmonary lesions. Our aim is to design a FAPI trimer, Trap-(FAPI)3, to optimize pharmacokinetics and evaluate whether this novel drug offers superior advantages over its monomer analogs in the imaging diagnosis and staging of pulmonary tumors.
- Conditions
- Lung Nodules
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
| Study group | Role | What they receive |
|---|---|---|
| patients with pulmonary nodules | Not described |
What is being measured
The primary outcome is the main question the study is designed to answer.
Diagnostic efficacy of Trap-(FAPI)3 probe for pulmonary nodules
sensitivity, specificity, accuracy, positive and negative predictive values, ROC curve analysis,
Measured: through study completion, an average of 1 year
Histologic Scores for Fibrotic
Paraffin section specimens were stained by using Masson trichrome for the histologic fibrosis score. Two pathologists graded the histologic slices from the most severe areas for fibrosis by using a semiquantitative scoring system. The fibrosis score was scored between 0 and 3 points as follows: 0: none (No fibrosis), 1: mild (Minimal fibrosis in submucosa or subserosa), 2: moderate (Increased submucosal fibrosis, septa into
muscularis propria and/or septa through muscularis propria, increase in subserosal collage), 3: severe (Significant transmural scar, marked subserosal collagen).
Measured: Completed within one week after surgery
Metabolic parameters
Total Lesion Glycolysis (TLG) of bowel lesions are measured on PET.
Measured: Completed within one week after PET examination
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted4 Mar 2026
- Study start1 Mar 2026 (estimated)
- Primary completion30 Dec 2027 (estimated)
- Study completion31 Dec 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Lung NodulesStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Case only
- Time perspective
- Prospective
- Enrolment
- 50 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Daping Hospital and the Research Institute of Surgery of the Third Military Medical University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Xiao Chen, Daping Hospital and the Research Institute of Surgery of the Third Military Medical University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07448441
- Sponsor's protocol ID
- 2026033
- Status last verified
- Mar 2026
- First submitted
- 23 Feb 2026
- Last updated
- 4 Mar 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 4 Mar 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Clinical Study of Trap-(FAPI)3 PET Imaging in the Diagnosis of Pulmonary Nodules
- ClinicalTrials.gov ID
- NCT07448441
- Acronym / sponsor ID
- 2026033
- Conditions
- Lung Nodules
- Study type
- Observational
- Recruitment status
- Not yet recruiting
- Enrolment
- 50 participants (estimated)
- Lead sponsor
- Daping Hospital and the Research Institute of Surgery of the Third Military Medical UniversityUniversity, hospital or other
- Study start
- 1 Mar 2026 (estimated)
- Primary completion
- 30 Dec 2027 (estimated)
- Study completion
- 31 Dec 2027 (estimated)
- First posted
- 4 Mar 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The excellent tumor-targeting efficacy of FAP has been confirmed by multiple clinical studies. The results unequivocally establish FAPI as a tumor-targeting ligand with significant potential, demonstrating important application prospects in translational oncology. However, its therapeutic effects remain under investigation. An ideal radiopharmaceutical for cancer treatment should possess outstanding targeting specificity and relatively prolonged tumor retention time. Previous studies have shown that radiolabeled FAPI variants (FAPI-04 and FAPI-46) rapidly and satisfactorily accumulate in tumors, while exhibiting low physiological uptake in normal tissues. However, prior FAP-related tracers demonstrated relatively short retention times in small pulmonary lesions. Our aim is to design a FAPI trimer, Trap-(FAPI)3, to optimize pharmacokinetics and evaluate whether this novel drug offers superior advantages over its monomer analogs in the imaging diagnosis and staging of pulmonary tumors.
Detailed description
Positron Emission Tomography (PET) is a functional imaging technology for the diagnosis and monitoring of tumors. The clinical applications of PET in malignant tumors, including staging, response evaluation, and efficacy prediction, provide attractive semi-quantitative biomarkers for clinical and research platforms. Understanding the advantages and limitations of fundamental imaging science and imaging modalities is crucial for optimizing research evaluations. With the widespread use of functional techniques and the development of novel PET biomarkers, PET research evaluations will be further improved.
The field of oncology has undergone a revolution due to molecular imaging, which evaluates tumor biology, while traditional radiological imaging focuses on morphological anatomy. Molecular imaging employs non-invasive visualization of physiological or pathological processes at the cellular or subcellular level. Positron Emission Tomography/Computed Tomography (PET/CT) is a hybrid imaging tool that provides complementary information on both function and structure. [18F]Fluorodeoxyglucose (FDG), first developed in the late 1970s as a tracer for brain metabolism, is now the most widely used PET tracer with applications in both oncological and non-oncological pathways. Although its clinical utility is undeniable, FDG uptake serves as a surrogate indicator for glucose transport/metabolism and is not specific to malignant tumors. The diagnostic accuracy of FDG for pulmonary nodules has long been a challenge, as tumor cells are scarce, solid components are minimal, and mucinous components are excessive. Multiple factors can lead to low uptake or no uptake of pulmonary nodules.
Through continuous exploration of cellular targets, fibroblast-activating protein (FAP) was identified. Cancer-associated fibroblasts are present in numerous tumors, particularly those with strong fibroblast proliferation responses, such as breast cancer, colorectal cancer, pancreatic cancer, prostate cancer, and lung cancer. Consequently, FAP expression is detected in over 90% of epithelial tumors. To date, FAP expression has been reported to correlate with poor tumor prognosis, as observed in colorectal cancer, pancreatic cancer, hepatocellular carcinoma, and ovarian cancer. Although further research is required, this advantage positions cancer-associated fibroblasts as an ideal target for antitumor therapy. In practical applications, low FAP expression in fibroblasts or healthy tissues facilitates imaging of pathological changes with low background signals.
Cancer-associated fibroblasts (CAFs) are key components of the tumor microenvironment, accounting for over half of the mass in various types of tumors. Previous studies have demonstrated that CAFs play significant roles in tumor growth, immunosuppression, and cancer invasion. Consequently, CAFs may emerge as a novel therapeutic target for lung tumor diagnosis and treatment. Fibroblast-activating protein (FAP) is overexpressed in CAFs of multiple epithelial cancers but weakly expressed in healthy tissues, making it an attractive target in cancer research. In recent years, molecular imaging targeting FAP has been extensively explored in the field of tumor diagnosis.
The excellent tumor-targeting efficacy of FAP has been confirmed by multiple clinical studies. The results unequivocally establish FAPI as a tumor-targeting ligand with significant potential, demonstrating important application prospects in translational oncology. However, its therapeutic effects remain under investigation. An ideal radiopharmaceutical for cancer treatment should possess outstanding targeting specificity and relatively prolonged tumor retention time. Previous studies have shown that radiolabeled FAPI variants (FAPI-04 and FAPI-46) rapidly and satisfactorily accumulate in tumors, while exhibiting low physiological uptake in normal tissues. However, prior FAP-related tracers demonstrated relatively short retention times in small pulmonary lesions. Our aim is to design a FAPI trimer, Trap-(FAPI)3, to optimize pharmacokinetics and evaluate whether this novel drug offers superior advantages over its monomer analogs in the imaging diagnosis and staging of pulmonary tumors.
Study design
- Observational model
- Case only
- Time perspective
- Prospective
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| patients with pulmonary nodules | – | – |
Who may qualify
- Ages
- 18 to 65 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- The subjects we selected are adults who are not restricted by gender. Fordetails, please refer to the "EligibilityCriteria" colymn.
Key inclusion criteria (4 listed)
- 1) Patients aged over 18 years with no gender restriction;
- 2) Patients with radiographic findings of pulmonary nodules;
- 3) Patients eligible for Trap-(FAPI)3 PET examination;
- 4) Written informed consent signed by the subject or their legal guardian.
Key exclusion criteria (6 listed)
- 1) Patients who have received antitumor therapy prior to PET/CT scanning;
- 2) Patients with severe diseases that cannot tolerate PET/CT scanning;
- 3) Alternative subjects with contraindications to PET/CT scanning;
- 4) Radiation exposure exceeding 50 mSv dose in the past year;
- 5) Alternative subjects who underwent major surgery within the past 3 months; those who received experimental drugs or devices (with unclear efficacy or safety) within the past 1 month;
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Diagnostic efficacy of Trap-(FAPI)3 probe for pulmonary nodules
Time frame: through study completion, an average of 1 year
sensitivity, specificity, accuracy, positive and negative predictive values, ROC curve analysis,
Histologic Scores for Fibrotic
Time frame: Completed within one week after surgery
Paraffin section specimens were stained by using Masson trichrome for the histologic fibrosis score. Two pathologists graded the histologic slices from the most severe areas for fibrosis by using a semiquantitative scoring system. The fibrosis score was scored between 0 and 3 points as follows: 0: none (No fibrosis), 1: mild (Minimal fibrosis in submucosa or subserosa), 2: moderate (Increased submucosal fibrosis, septa into muscularis propria and/or septa through muscularis propria, increase in subserosal collage), 3: severe (Significant transmural scar, marked subserosal collagen).
Metabolic parameters
Time frame: Completed within one week after PET examination
Total Lesion Glycolysis (TLG) of bowel lesions are measured on PET.
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 4 Mar 2026.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Lung Nodules, run by Daping Hospital and the Research Institute of Surgery of the Third Military Medical University at 1 site in China.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 4 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: opening soon, as of the sponsor's last update on 4 Mar 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in China. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Diagnostic efficacy of Trap-(FAPI)3 probe for pulmonary nodules (time frame: through study completion, an average of 1 year). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 4 Mar 2026.